Effect of pulsing electromagnetic fields on DNA synthesis in mammalian cells in culture

Summary DNA synthesis in Chinese hamster V79 cells was significantly enhanced when they were exposed to weak, pulsing electromagnetic fields generated by specific combinations of the pulse width (25s), frequency (10, 100 Hz) and magnetic intensity (2×10^–5 8×10^–5T). Conversely the DNA synthesis of cells in the fields at 4×10^–4 T was repressed to 80% of that in controls not exposed to the fields.This work was supported by Kaken Pharmaceutical Co., Ltd, Tokyo, Japan, and in part by a Grant-in-Aid from the Ministry of Education, Science and Culture of Japan and from the Foundation for Life Science Promotion Tokyo, Japan to I.K.     

Influence of pulsing electromagnetic field on the frequency of sister-chromatid exchanges in cultured mammalian cells

Exposures of Chinese hamster cells to pulsing electromagnetic field (PEMF) with 0.18-2.5 mT did not influence the baseline frequency of sister-chromatid exchanges (SCE). The results suggest that PEMF with the magnetic intensity examined does not interfere with DNA replication nor produce DNA lesions, thereby leading to an increased frequency of SCE.     

Influence of pulsing electromagnetic field on the frequency of sister-chromatid exchanges in cultured mammalian cells

Summary Exposure of Chinese hamster cells to pulsing electromagnetic field (PEMF) with 0.18–2.5 mT did not influence the baseline frequency of sister-chromatid exchanges (SCE). The results suggest that PEMF with the magnetic intensity examined does not interfere with DNA replication nor produce DNA lesions, thereby leading to an increased frequency of SCE.     

Y-family DNA polymerases in mammalian cells

Eukaryotic genomes are replicated with high fidelity to assure the faithful transmission of genetic information from one generation to the next. The accuracy of replication relies heavily on the ability of replicative DNA polymerases to efficiently select correct nucleotides for the polymerization reaction and, using their intrinsic exonuclease activities, to excise mistakenly incorporated nucleotides. Cells also possess a variety of specialized DNA polymerases that, by a process called translesion DNA synthesis (TLS), help overcome replication blocks when unrepaired DNA lesions stall the replication machinery. This review considers the properties of the Y-family (a subset of specialized DNA polymerases) and their roles in modulating spontaneous and genotoxic-induced mutations in mammals. We also review recent insights into the molecular mechanisms that regulate PCNA monoubiquitination and DNA polymerase switching during TLS and discuss the potential of using Y-family DNA polymerases as novel targets for cancer prevention and therapy.     

Effect of low density lipoprotein on proteoglycan synthesis by aorta cells in culture

Summary Increasing the content of human serum low density lipoprotein in the growth medium led to greater incorporation of³⁵S-sulfate into proteoglycan (mostly into dermatan sulfate) by primary aorta cells but did not affect similar incorporation by fibroblast cells. These results suggest a mechanism which can explain the increased deposition of lipid in aorta due to hyperlipidemia.Acknowledgements. This work was supported by a Fort Polk-American Heart Association-Louisiana, Inc. Research Award.     

Effect of low density lipoprotein on proteoglycan synthesis by aorta cells in culture.

Increasing the content of human serum low density lipoprotein in the growth medium led to greater incorporation of 35S-sulfate into proteoglycan (mostly into dermatan sulfate) by primary aorta cells but did not affect similar incorporation by fibroblast cells. These results suggest a mechanism which can explain the increased deposition of lipid in aorta due to hyperlipidemia.     

Effects of butyrate and insulin and their interaction on the DNA synthesis of rumen epithelial cells in culture

Summary Rumen epithelial cells (REC) were incubated in the presence of various concentrations of butyrate or insulin or with both of them, to obtain information on their effect on the DNA synthesis of cultured cells. The 24-h values of³H-thymidine incorporation into cellular DNA were measured in the presence of butyrate, insulin or butyrate plus insulin. While butyrate reduced DNA synthesis, insulin produced an increase over the control. Combined butyrate plus insulin treatment influenced the incorporation of label in accordance with the relative proportion of these two substances.     

Effects of butyrate and insulin and their interaction on the DNA synthesis of rumen epithelial cells in culture

Rumen epithelial cells (REC) were incubated in the presence of various concentrations of butyrate or insulin or with both of them, to obtain information on their effect on the DNA synthesis of cultured cells. The 24-h values of 3H-thymidine incorporation into cellular DNA were measured in the presence of butyrate, insulin or butyrate plus insulin. While butyrate reduced DNA synthesis, insulin produced an increase over the control. Combined butyrate plus insulin treatment influenced the incorporation of label in accordance with the relative proportion of these two substances.     

Effect of the growth-promoting alpha-globulin (GPAG) on in vitro incorporation of exogenous DNA into mammalian cells

Summary The uptake of exogenous³H-DNA by mammalian cells is increased in the presence of a specific serum protein complex — growth-promoting alpha-globulin (GPAG).³H-DNA is retained in the cell nucleus in a quantity 3 times higher than for control cultures without GPAG even after 47h of additional cultivation in the medium without³H-DNA.     

DNA synthesis in glial cells during nerve regeneration

Zusammenfassung Autoradiographie von Gliazellen, welche regenerierende motorische Nervenzellen umgeben, ergab eine stark erhöhte DNA-Synthese in den Gliazellen zwischen dem zweiten und sechsten Tag nach dem Nervenschaden. Morphologisch erscheinen typische Gliaveränderungen mit hochgradiger Hypertrophie der Astrocyten in der zweiten und dritten Woche nach der Operation.     

Studies on DNA methylase activity in mammalian tissue

Resumen Para aislar nucleo de mamíferos que contienen DNA metilasa actividad se utilizó como medio homogenizante 0.25M sucrosa-1×10^–2 M EDTA. Hígado de rata y el hepatoma de Reuber demostraron cantidad equivalente de actividad enzimática. Se observó aproximadamente 100% de inhibición con amoníaco 0.15M, los iones de Mg no mostraron efecto.     

Cation inhibition of DNA synthesis in mammary epithelial cells in vitro

Zusammenfassung Lithium- und Ammoniumionen verhindern den Anfang der DNA-Synthese im Milchdrüsenepithel in vitro. Die Replikation von DNA, nach dem Anfang derS-Periode, wird jedoch nicht verhindert. Diese spezifische Verhinderung der Dauer derG ₁-Periode durch die ionale Umgebung zeigt, dass Mechanismen, die für die Regulierung der Zellproduktion wichtig sind, während derG ₁-Periode intervenieren.

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This work was supported in part by grant No. CA 10268 from the U.S. Public Health Service.     

Differential sensitivity to ethidium bromide of replicative DNA synthesis and bleomycin-induced unscheduled DNA synthesis in permeable mouse sarcoma cells

Replicative DNA synthesis in permeable mouse sarcoma cells was more sensitive to ethidium bromide (EtBr) than bleomycin-induced unscheduled DNA synthesis (UDS). A similar difference in sensitivity to EtBr was observed between DNA polymerases alpha and beta. The difference in sensitivity to EtBr of replicative DNA synthesis and UDS in the present system seems to reflect mainly the sensitivity difference between DNA polymerases alpha and beta.